List of variants in gene CSF3R reported as uncertain significance by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_000760.4(CSF3R):c.2334G>A (p.Ala778=)	rs116118817	0.00154
NM_000760.4(CSF3R):c.1856T>C (p.Leu619Ser)	rs141619366	0.00115
NM_000760.4(CSF3R):c.355G>A (p.Ala119Thr)	rs142999683	0.00089
NM_000760.4(CSF3R):c.272A>G (p.His91Arg)	rs148307285	0.00026
NM_000760.4(CSF3R):c.1457C>T (p.Thr486Met)	rs759506026	0.00016
NM_000760.4(CSF3R):c.1665G>T (p.Gly555=)	rs139705992	0.00015
NM_000760.4(CSF3R):c.1864+12C>T	rs368290894	0.00014
NM_000760.4(CSF3R):c.2072C>T (p.Pro691Leu)	rs183614500	0.00013
NM_000760.4(CSF3R):c.1028G>A (p.Arg343Gln)	rs369185176	0.00009
NM_000760.4(CSF3R):c.1027C>T (p.Arg343Trp)	rs752325760	0.00004
NM_000760.4(CSF3R):c.1101G>C (p.Arg367=)	rs1447131096	0.00004
NM_000760.4(CSF3R):c.722C>T (p.Ala241Val)	rs199991273	0.00004
NM_000760.4(CSF3R):c.2069C>T (p.Thr690Met)	rs764345289	0.00003
NM_000760.4(CSF3R):c.826G>A (p.Glu276Lys)	rs201037400	0.00003
NM_000760.4(CSF3R):c.1325C>T (p.Pro442Leu)	rs948001842	0.00002
NM_000760.4(CSF3R):c.998-3C>T	rs753747584	0.00002
NM_000760.4(CSF3R):c.1286-3C>T	rs778391319	0.00001
NM_000760.4(CSF3R):c.1624T>C (p.Trp542Arg)	rs763748002	0.00001
NM_000760.4(CSF3R):c.1795C>A (p.His599Asn)	rs750968883	0.00001
NM_000760.4(CSF3R):c.2192G>A (p.Gly731Glu)	rs1553151543	0.00001
NM_000760.4(CSF3R):c.2428G>A (p.Asp810Asn)	rs567871402	0.00001
NM_000760.4(CSF3R):c.392G>A (p.Cys131Tyr)	rs777701371	0.00001
NM_000760.4(CSF3R):c.40C>G (p.Leu14Val)	rs752051152	0.00001
NM_000760.4(CSF3R):c.491G>A (p.Arg164Gln)	rs754336092	0.00001
NM_000760.4(CSF3R):c.820C>T (p.Arg274Cys)	rs759587248	0.00001
NM_000760.4(CSF3R):c.1262C>A (p.Pro421Gln)	rs776379864
NM_000760.4(CSF3R):c.1282A>G (p.Arg428Gly)	rs2124118241
NM_000760.4(CSF3R):c.1666A>G (p.Lys556Glu)	rs1650463783
NM_000760.4(CSF3R):c.1867G>T (p.Gly623Trp)	rs1437330772
NM_000760.4(CSF3R):c.1870T>A (p.Ser624Thr)
NM_000760.4(CSF3R):c.2130G>C (p.Glu710Asp)	rs370491074
NM_000760.4(CSF3R):c.326T>C (p.Leu109Pro)	rs1290014200
NM_000760.4(CSF3R):c.624G>T (p.Ala208=)	rs776543343

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